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T6016Maraviroc马拉维若；Celsentri；Selzentry；UK-427857
Maraviroc is a C-C Chemokine Receptor Type 5 (CCR5) antagonist, and for MIP-1α(IC50=3.3 nM), MIP-1β (IC50=7.2 nM) and RANTES(IC50=5.2 nM).Maraviroc inhibits HIV-1 entry via CCR5 coreceptor interaction.
价 格：￥电议型 号：T6016产 地：中国大陆
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T5S0285Cistanoside A肉苁蓉苷 A；肉苁蓉苷A
1. Cistanoside A possesses protective activities on CCl4 induced hepatotoxicity in mice, which is involved with increasing free radicals clearing activities, alleviating lipid-overoxidation damage, and improving respiratory chain function in mitochondria.
价 格：￥电议型 号：T5S0285产 地：中国大陆
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T5985Glycolic acid
Glycolic acid is an inhibitor of tyrosinase, suppressing melanin formation,and used in skincare products
价 格：￥电议型 号：T5985产 地：中国大陆
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T5885N-Acetyl-D-galactosamineGalNAc；2-乙酰胺基-2-脱氧-D-半乳糖
N-Acetyl-d-galactosamine (GalNAc) is a terminal essential amino sugar derived from galactose and forms the antigens of blood group A in humans.
价 格：￥电议型 号：T5885产 地：中国大陆
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T5858SertindoleLu 23-174；舍吲哚
Sertindole is an atypical antipsychotic that binds to dopamine D2 receptors and the serotonin (5-HT) receptor subtypes 5-HT1D, 5-HT2A, and 5-HT2C (Kds = 2.7, 20, 0.14, and 6 nM, respectively)
价 格：￥电议型 号：T5858产 地：中国大陆
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T5857Trametinib (DMSO solvate)Trametinib dimethyl sulfoxide；JTP-74057 (DMSO solvate)；GSK-1120212 (DMSO so
Trametinib DMSO solvate is a Highly Potent and Selective MEK Inhibitor that specifically inhibits MEK1/2(IC50 :2 nM)
价 格：￥电议型 号：T5857产 地：中国大陆
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T5856Barnidipine hydrochloride盐酸巴尼地平；Mepirodipine (hydrochloride)；YM-09730-5 hydrochloride
Barnidipine hydrochloride is a dihydropyridine calcium channel blocker that has an IC50 value of 0.35 nM in potassium-induced tonic contraction of pig coronary artery
价 格：￥电议型 号：T5856产 地：中国大陆
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T5855Edrophonium chloride
Edrophonium chloride is an acetylcholinesterase (AChE) inhibitor that is known to prevent the breakdown of the neurotransmitter acetylcholine by binding specifically to its catalytic site.
价 格：￥电议型 号：T5855产 地：中国大陆
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T5854AM580CD336；NSC608001；Ro 40-6055
AM580 is a retinoic acid receptor agonist that is selective for RARα( IC50 : 8 nM )
价 格：￥电议型 号：T5854产 地：中国大陆
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T5853Rubitecan鲁比特康；9-Nitrocamptothecin；RFS 2000
Rubitecan is a DNA topoisomerase I inhibitor. It inhibits DNA topoisomerase I and increases the fraction of supercoiled DNA in a cell-free assay in a concentration-dependent manner.Rubitecan is a semisynthetic agent related to camptothecin with potent ant
价 格：￥电议型 号：T5853产 地：中国大陆
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T5852Canthaxanthin角黄素；斑蝥黄；all-trans-Canthaxanthin；E 161g
Canthaxanthin is a red-orange carotenoid that belongs to the xanthophyll group. This naturally occurring pigment is present in bacteria, algae and some fungi.
价 格：￥电议型 号：T5852产 地：中国大陆
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T5851N-Methylpyrrolidone1-Methyl-2-pyrrolidinone；N-甲基吡咯烷酮
N-Methylpyrrolidone (1-Methyl-2-pyrrolidinone) is a five-membered cyclic amide. N-Methylpyrrolidone is a widely used industrial organic polar solvent in the manufacture of adhesives, paints, fuels, and pharmaceuticals.
价 格：￥电议型 号：T5851产 地：中国大陆
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T5850BenzamilBenzamil (hydrochloride)
Benzamil is an epithelial sodium channel (ENaC) blocker that inhibits sodium transport from (IC50 = 4 nM) and binds to (Kd = 5 nM) bovine kidney cortex membrane vesicles.
价 格：￥电议型 号：T5850产 地：中国大陆
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T5785MALTOTETRAOSEα-1,4-Tetraglucose；Amylotetraose；Fujioligo 450；麦芽四糖
MALTOTETRAOSE are potent inhibitors of TNF-α-induced intercellular adhesion molecule-1 (ICAM-1) expression, maltotetraose may be beneficial in the suppression of early atherosclerosis development.
价 格：￥电议型 号：T5785产 地：中国大陆
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T5585AM-92016 hydrochloride
AM-92016 is a specific blocker of rectifier potassium current. AM-92016 delays rectifier potassium channel and repolarizes the membrane thereby restricting the duration of the nerve impulse.
价 格：￥电议型 号：T5585产 地：中国大陆
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T5512JNJ16259685.TN.T 16259685
JNJ16259685 is a selective mGluR1 antagonist, and inhibits the synaptic activation of mGluR1 in a concentration-dependent manner with IC50 of 19 nM.
价 格：￥电议型 号：T5512产 地：中国大陆
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T5485OSU-T315OSU-T315 (1,5-regioisomer)；ILK-IN-2
OSU-T315 (1,5-regioisomer) is a ILK inhibitor.
价 格：￥电议型 号：T5485产 地：中国大陆
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T5465PF-5274857PF5274857；PF-5274857 freebase；PF 5274857
PF-5274857 is an effective and selective hedgehog signaling pathway inhibitor (IC50: 5.8 nM and a Ki: 4.6 nM). PF-5274857 is a potentially attractive clinical candidate for the treatment of tumor types including brain tumors and brain metastasis driven by
价 格：￥电议型 号：T5465产 地：中国大陆
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T5413ML216CID-49852229
ML-216 is a small molecule inhibitor of BLM helicase (IC50: 1.8 μM). It showed 28-fold selective against the related helicases RECQ1, RECQ5, and E. coli UvrD (IC50s > 50 μM).
价 格：￥电议型 号：T5413产 地：中国大陆
